G. Bosscher et al., POLYMERIZATION OF AN ACETOXYVINYL SUBSTITUTED CHLOROCYCLOPHOSPHAZENE, Journal of inorganic and organometallic polymers, 7(1), 1997, pp. 19-34
The vinyl acetate derivative, (alpha-acetoxyvinyl)tetrachlorocyclotrip
hosphazene (1), has been used in radical homopolymerization and copoly
merization reactions with methyl methacrylate, (MMA) and styrene. The
1,1-disubstituted olefin did not undergo radical homopolymerization. C
opolymers derived from MMA and 1 contained only low amounts (<2 mol%)
of 1. A maximum incorporation of 20 mol% of phosphazene monomer was ac
hieved with styrene as comonomer. The data obtained in low-and high-co
nversion copolymerizations with styrene were used to calculate the mon
omer reactivity ratios. The results of the calculations show that the
terminal model is not operative. Calculation for the penultimate model
with r(2) = 0 resulted in r(1) and r(1)' values of 2.8 +/- 0.2 and 0.
7 +/- 0.1, respectively. For the hypothetical homopolymer of 1 a T-g v
alue of 441 K was calculated. All the copolymers with styrene exhibit
flame-retardant properties.